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Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma

The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during...

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Autores principales: Rasche, L, Alapat, D, Kumar, M, Gershner, G, McDonald, J, Wardell, C.P, Samant, R, Van Hemert, R, Epstein, J, Williams, A.F, Thanendrarajan, S, Schinke, C, Bauer, M, Ashby, C, Tytarenko, R.G, van Rhee, F, Walker, B.A, Zangari, M, Barlogie, B, Davies, F.E, Morgan, G.J, Weinhold, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586541/
https://www.ncbi.nlm.nih.gov/pubmed/30573775
http://dx.doi.org/10.1038/s41375-018-0329-0
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author Rasche, L
Alapat, D
Kumar, M
Gershner, G
McDonald, J
Wardell, C.P
Samant, R
Van Hemert, R
Epstein, J
Williams, A.F
Thanendrarajan, S
Schinke, C
Bauer, M
Ashby, C
Tytarenko, R.G
van Rhee, F
Walker, B.A
Zangari, M
Barlogie, B
Davies, F.E
Morgan, G.J
Weinhold, N
author_facet Rasche, L
Alapat, D
Kumar, M
Gershner, G
McDonald, J
Wardell, C.P
Samant, R
Van Hemert, R
Epstein, J
Williams, A.F
Thanendrarajan, S
Schinke, C
Bauer, M
Ashby, C
Tytarenko, R.G
van Rhee, F
Walker, B.A
Zangari, M
Barlogie, B
Davies, F.E
Morgan, G.J
Weinhold, N
author_sort Rasche, L
collection PubMed
description The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during first-line or salvage therapy, for whom MRD flow-cytometry and the two imaging modalities positron-emission-tomography (PET) and diffusion-weighted magnetic resonance imaging (DW-MRI) were performed at the onset of CR. Residual focal lesions (FLs), detectable in 24% of first-line patients, were associated with short progression-free survival (PFS), with DW-MRI detecting disease in more patients. In some patients, FLs were only PET-positive, indicating that the two approaches are complementary. Combining MRD and imaging improved prediction of outcome, with double-negative and double-positive features defining groups with excellent and dismal PFS, respectively. FLs were a rare event (12%) in first-line MRD-negative CR patients. In contrast, patients achieving an MRD-negative CR during salvage therapy frequently had FLs (50%). Multi-region sequencing and imaging in an MRD-negative patient showed persistence of spatially separated clones. In conclusion, we show that DW-MRI is a promising tool for monitoring residual disease that complements PET and should be combined with MRD.
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spelling pubmed-65865412019-06-21 Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma Rasche, L Alapat, D Kumar, M Gershner, G McDonald, J Wardell, C.P Samant, R Van Hemert, R Epstein, J Williams, A.F Thanendrarajan, S Schinke, C Bauer, M Ashby, C Tytarenko, R.G van Rhee, F Walker, B.A Zangari, M Barlogie, B Davies, F.E Morgan, G.J Weinhold, N Leukemia Article The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during first-line or salvage therapy, for whom MRD flow-cytometry and the two imaging modalities positron-emission-tomography (PET) and diffusion-weighted magnetic resonance imaging (DW-MRI) were performed at the onset of CR. Residual focal lesions (FLs), detectable in 24% of first-line patients, were associated with short progression-free survival (PFS), with DW-MRI detecting disease in more patients. In some patients, FLs were only PET-positive, indicating that the two approaches are complementary. Combining MRD and imaging improved prediction of outcome, with double-negative and double-positive features defining groups with excellent and dismal PFS, respectively. FLs were a rare event (12%) in first-line MRD-negative CR patients. In contrast, patients achieving an MRD-negative CR during salvage therapy frequently had FLs (50%). Multi-region sequencing and imaging in an MRD-negative patient showed persistence of spatially separated clones. In conclusion, we show that DW-MRI is a promising tool for monitoring residual disease that complements PET and should be combined with MRD. 2018-12-20 2019-07 /pmc/articles/PMC6586541/ /pubmed/30573775 http://dx.doi.org/10.1038/s41375-018-0329-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Rasche, L
Alapat, D
Kumar, M
Gershner, G
McDonald, J
Wardell, C.P
Samant, R
Van Hemert, R
Epstein, J
Williams, A.F
Thanendrarajan, S
Schinke, C
Bauer, M
Ashby, C
Tytarenko, R.G
van Rhee, F
Walker, B.A
Zangari, M
Barlogie, B
Davies, F.E
Morgan, G.J
Weinhold, N
Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title_full Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title_fullStr Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title_full_unstemmed Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title_short Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
title_sort combination of flow cytometry and functional imaging for monitoring of residual disease in myeloma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586541/
https://www.ncbi.nlm.nih.gov/pubmed/30573775
http://dx.doi.org/10.1038/s41375-018-0329-0
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